Viviane L Ndam Ngoungoure1,2, Patricia Muñoz2, Yousef Tizabi3, Raul Valdes2, Paul Fewou Moundipa1, Juan Segura-Aguilar2. 1. Laboratory of Pharmacology and Toxicology, Department of Biochemistry, Faculty of Sciences, University of Yaoundé I, Cameroon. 2. Department of Molecular & Clinical Pharmacology, Faculty of Medicine, ICBM, University of Chile, Santiago, Chile. 3. Department of Pharmacology, Howard University College of Medicine, 520 W Street NW, Washington, DC 20059, USA.
Abstract
BACKGROUND/AIMS: Aminochrome, an endogenous compound formed during dopamine oxidation can induce neurotoxicity under certain aberrant conditions and induce Parkinson-like syndrome. Glutathione transferase M2 (GSTM2) activity of astrocytes by catalysing the conjugation of aminochrome with glutathione, can offer protection against aminochrome toxicity. Some medicinal toxicity through this plants may exert protective effect against aminochrome mechanism. METHODS: In the present study, extracts from plants native to Cameroon, such as Alchornea laxiflora (leaves), Dacryodes edulis (barks), Annona muricata (seeds), Annona senegalensis (barks) were evaluated for their protection against aminochrome-induced toxicity in human glioblastoma/ astrocytoma U373MG wild type and U373MGsiGT6 cells in which GSTM2 expression was 74% silenced. The cells were pre-incubated with the plant extracts for 2 hr before addition of aminochrome (75 μM) and measurement of cell death/viability by flow cytometry after 24 hr incubation. RESULTS: The extract of A. laxiflora (1 μg/ml), D. edulis (25 μg/ml), A. muricata (25 μg/ml) and A. senegalensis (25μg/ml) significantly decreased aminochrome-induced toxicity in U373siGST6 and U373MG cells. However, only A. laxiflora and A. muricata significantly increased the mitochondria membrane potential in U373siGST6 cells following aminochrome treatment. CONCLUSION: The results indicate that extracts of some Cameroon plants can provide protection against aminochrome-induced toxicity and mitochondria dysfunction in human glioblastoma/astrocytoma cells. Although further identification of active components of these extracts is needed, potential usefulness of these compounds in Parkinson's disease may be suggested.
BACKGROUND/AIMS: Aminochrome, an endogenous compound formed during dopamine oxidation can induce neurotoxicity under certain aberrant conditions and induce Parkinson-like syndrome. Glutathione transferase M2 (GSTM2) activity of astrocytes by catalysing the conjugation of aminochrome with glutathione, can offer protection against aminochrome toxicity. Some medicinal toxicity through this plants may exert protective effect against aminochrome mechanism. METHODS: In the present study, extracts from plants native to Cameroon, such as Alchornea laxiflora (leaves), Dacryodes edulis (barks), Annona muricata (seeds), Annona senegalensis (barks) were evaluated for their protection against aminochrome-induced toxicity in human glioblastoma/ astrocytoma U373MG wild type and U373MGsiGT6 cells in which GSTM2 expression was 74% silenced. The cells were pre-incubated with the plant extracts for 2 hr before addition of aminochrome (75 μM) and measurement of cell death/viability by flow cytometry after 24 hr incubation. RESULTS: The extract of A. laxiflora (1 μg/ml), D. edulis (25 μg/ml), A. muricata (25 μg/ml) and A. senegalensis (25μg/ml) significantly decreased aminochrome-induced toxicity in U373siGST6 and U373MG cells. However, only A. laxiflora and A. muricata significantly increased the mitochondria membrane potential in U373siGST6 cells following aminochrome treatment. CONCLUSION: The results indicate that extracts of some Cameroon plants can provide protection against aminochrome-induced toxicity and mitochondria dysfunction in human glioblastoma/astrocytoma cells. Although further identification of active components of these extracts is needed, potential usefulness of these compounds in Parkinson's disease may be suggested.
Authors: Luigi Zecca; Ruggero Fariello; Peter Riederer; David Sulzer; Alberto Gatti; Davide Tampellini Journal: FEBS Lett Date: 2002-01-16 Impact factor: 4.124
Authors: Cleonice Creusa Santos; Thyago R Cardim-Pires; Liana Shvachiy; Luis Arturo Fonseca-Fonseca; Patricia Muñoz; Áurea Maria A N Almeida; Ana Carla S Costa; Jéssica Teles-Souza; Estael Ochoa-Rodríguez; Maria de Fátima Dias Costa; Fernando L Palhano; Juan Segura-Aguilar; Deyse B Barbosa; Mayra R do Bomfim; Manoelito C Dos Santos Junior; Franco Henrique A Leite; Samuel Silva da Rocha Pita; Silvia Lima Costa; Yanier Núñez-Figueredo; Tiago Fleming Outeiro; Débora Foguel; Victor Diogenes Amaral Silva Journal: Neurotox Res Date: 2022-08-23 Impact factor: 3.978